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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1446958Generated: October 25, 2026

2,3-Butanediol → N-(4,5-Dimethyl-1,3-dioxolan-2-YL)-N-methyl-2-chloroacetamide

https://huagongshe.com/reaction/1446958

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-ButanediolHCID 262—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant2-Chloro-N-(2,2-dimethoxyethyl)-N-methylacetamideHCID 12850700—
SolventMethanolHCID 887—
ProductN-(4,5-Dimethyl-1,3-dioxolan-2-YL)-N-methyl-2-chloroacetamideHCID 20551717—

Reaction Conditions

Temperature110 °C

Reaction Steps

N-(2,2-Dimethoxyethyl)-N-methyl-2-chloroacetamide (97.8 grams; 0.5 mole), 2,3-butanediol (45 grams) and 0.2 grams p-toluenesulfonic acid were charged into a glass reaction vessel fitted with a mechanical stirrer, thermometer, distilling head and condenser. The reaction mixture was heated at about 90° C. to 100° for a period of 5 hours. Little reaction occurred as shown by the absence of methanol distilled. The reaction mixture was then heated at about 110° C., for about 2 hours at atmospheric pressure, then 1 hour at reduced pressure. Under these more rigorous conditions, methanol was formed and was distilled off. At the conclusion of the reaction, the reaction mixture was distilled and the fraction boiling at 127° C. to 130° C. at 0.55 mm Hg was the desired product N-(4,5-dimethyl-1,3-dioxolan-2-yl)-N-methyl-2-chloroacetamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04314840
Source datasetuspto-grants-1982_02
ORD IDord-df5f30e24d8848b2aa8a27dab98251d0
Source noteuspto-grants-1982_02